{{Rsnum
|rsid=33978907
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5225488
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33978907
|variant=0382
}}{{ClinVar
|rsid=33978907
|Reversed=1
|FwdREF=T
|FwdALT=A,C
|REF=A
|ALT=G,T
|RSPOS=5246718
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246718A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000030000.1
|CLNDBN=Beta thalassemia intermedia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0472767:191189009
|CLNSRC=GTR
|CLNSRCID=GTR000500319
|Disease=Beta thalassemia intermedia
}}{{PMID Auto
|PMID=1787101
|Title=A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
}}

{{PMID Auto
|PMID=2458145
|Title=Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
}}

{{PMID Auto
|PMID=4018033
|Title=Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human beta-globin gene.
|OA=1
}}

{{PMID Auto
|PMID=12709369
|Title=Rapid detection of beta-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis.
}}

{{PMID Auto
|PMID=15315795
|Title=Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
}}

{{PMID Auto
|PMID=21119755
|Title=Profiling beta-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes.
|OA=1
}}